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Sex differences in dementia with Lewy bodies: an imaging study of neurotransmission pathways

Purpose Dementia with Lewy bodies (DLB) is characterized by a wide clinical and biological heterogeneity, with sex differences reported in both clinical and pathologically confirmed DLB cohorts. No research evidence is available on sex differences regarding molecular neurotransmission. This study ai...

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Published in:European journal of nuclear medicine and molecular imaging 2023-06, Vol.50 (7), p.2036-2046
Main Authors: Boccalini, Cecilia, Nicastro, Nicolas, Peretti, Debora Elisa, Caminiti, Silvia Paola, Perani, Daniela, Garibotto, Valentina
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container_title European journal of nuclear medicine and molecular imaging
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creator Boccalini, Cecilia
Nicastro, Nicolas
Peretti, Debora Elisa
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Perani, Daniela
Garibotto, Valentina
description Purpose Dementia with Lewy bodies (DLB) is characterized by a wide clinical and biological heterogeneity, with sex differences reported in both clinical and pathologically confirmed DLB cohorts. No research evidence is available on sex differences regarding molecular neurotransmission. This study aimed to assess whether sex can influence neurotransmitter systems in patients with probable DLB (pDLB). Methods We included 123 pDLB patients (male/female: 77/46) and 78 control subjects (male/female: 34/44) for comparison, who underwent 123 I-FP-CIT SPECT imaging. We assessed sex differences in the dopaminergic activity of the nigrostriatal and mesolimbic systems using regional-based and voxel-wise analyses of 123 I-FP-CIT binding. We tested whether sex-specific binding alterations would also pertain to the serotoninergic and noradrenergic systems by applying spatial correlation analyses. We applied molecular connectivity analyses to assess potential sex differences in the dopaminergic pathways. Results We found comparable 123 I-FP-CIT binding decreases in the striatum for pDLB males and females compared to controls. However, pDLB females showed lower binding in the extrastriatal projections of the nigrostriatal and mesolimbic dopaminergic systems compared to pDLB males. According to the spatial correlation analysis, sex-specific molecular alterations were also associated with serotonergic and noradrenergic systems. Nigrostriatal and mesolimbic systems’ connectivity was impaired in both groups, with males showing local alterations and females presenting long-distance disconnections between subcortical and cortical regions. Conclusions Sex-specific differences in 123 I-FP-CIT binding were found in our cohort, namely, a trend for lower 123 I-FP-CIT binding in females, significant in the presence of a pDLB diagnosis. pDLB females showed also different patterns of connectivity compared to males, mostly involving extrastriatal regions. The results suggest the presence of a sex-related regional vulnerability to alpha-synuclein pathology, possibly complicated also by the higher prevalence of Alzheimer’s disease co-pathology in females, as previously reported in pDLB populations.
doi_str_mv 10.1007/s00259-023-06132-4
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No research evidence is available on sex differences regarding molecular neurotransmission. This study aimed to assess whether sex can influence neurotransmitter systems in patients with probable DLB (pDLB). Methods We included 123 pDLB patients (male/female: 77/46) and 78 control subjects (male/female: 34/44) for comparison, who underwent 123 I-FP-CIT SPECT imaging. We assessed sex differences in the dopaminergic activity of the nigrostriatal and mesolimbic systems using regional-based and voxel-wise analyses of 123 I-FP-CIT binding. We tested whether sex-specific binding alterations would also pertain to the serotoninergic and noradrenergic systems by applying spatial correlation analyses. We applied molecular connectivity analyses to assess potential sex differences in the dopaminergic pathways. Results We found comparable 123 I-FP-CIT binding decreases in the striatum for pDLB males and females compared to controls. However, pDLB females showed lower binding in the extrastriatal projections of the nigrostriatal and mesolimbic dopaminergic systems compared to pDLB males. According to the spatial correlation analysis, sex-specific molecular alterations were also associated with serotonergic and noradrenergic systems. Nigrostriatal and mesolimbic systems’ connectivity was impaired in both groups, with males showing local alterations and females presenting long-distance disconnections between subcortical and cortical regions. Conclusions Sex-specific differences in 123 I-FP-CIT binding were found in our cohort, namely, a trend for lower 123 I-FP-CIT binding in females, significant in the presence of a pDLB diagnosis. pDLB females showed also different patterns of connectivity compared to males, mostly involving extrastriatal regions. The results suggest the presence of a sex-related regional vulnerability to alpha-synuclein pathology, possibly complicated also by the higher prevalence of Alzheimer’s disease co-pathology in females, as previously reported in pDLB populations.</description><identifier>ISSN: 1619-7070</identifier><identifier>EISSN: 1619-7089</identifier><identifier>DOI: 10.1007/s00259-023-06132-4</identifier><identifier>PMID: 36826477</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Alzheimer's disease ; Binding ; Cardiology ; Correlation analysis ; Dementia ; Dementia disorders ; Dopamine receptors ; Female ; Females ; Gender differences ; Heterogeneity ; Humans ; Imaging ; Lewy bodies ; Lewy Body Disease - diagnostic imaging ; Male ; Males ; Medical imaging ; Medicine ; Medicine &amp; Public Health ; Mesolimbic system ; Neostriatum ; Neural networks ; Neurodegenerative diseases ; Neurology ; Neurotransmission ; Norepinephrine ; Nuclear Medicine ; Oncology ; Original ; Original Article ; Orthopedics ; Pathology ; Radiology ; Sex Characteristics ; Sex differences ; Single photon emission computed tomography ; Synuclein ; Tomography, Emission-Computed, Single-Photon - methods ; Tropanes</subject><ispartof>European journal of nuclear medicine and molecular imaging, 2023-06, Vol.50 (7), p.2036-2046</ispartof><rights>The Author(s) 2023</rights><rights>2023. The Author(s).</rights><rights>The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-f4f8cf771bf6b93ff95e9d35cca0b8cbfb9165cdce8c986949276693edac75d63</citedby><cites>FETCH-LOGICAL-c475t-f4f8cf771bf6b93ff95e9d35cca0b8cbfb9165cdce8c986949276693edac75d63</cites><orcidid>0000-0003-2422-698X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36826477$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Boccalini, Cecilia</creatorcontrib><creatorcontrib>Nicastro, Nicolas</creatorcontrib><creatorcontrib>Peretti, Debora Elisa</creatorcontrib><creatorcontrib>Caminiti, Silvia Paola</creatorcontrib><creatorcontrib>Perani, Daniela</creatorcontrib><creatorcontrib>Garibotto, Valentina</creatorcontrib><title>Sex differences in dementia with Lewy bodies: an imaging study of neurotransmission pathways</title><title>European journal of nuclear medicine and molecular imaging</title><addtitle>Eur J Nucl Med Mol Imaging</addtitle><addtitle>Eur J Nucl Med Mol Imaging</addtitle><description>Purpose Dementia with Lewy bodies (DLB) is characterized by a wide clinical and biological heterogeneity, with sex differences reported in both clinical and pathologically confirmed DLB cohorts. No research evidence is available on sex differences regarding molecular neurotransmission. This study aimed to assess whether sex can influence neurotransmitter systems in patients with probable DLB (pDLB). Methods We included 123 pDLB patients (male/female: 77/46) and 78 control subjects (male/female: 34/44) for comparison, who underwent 123 I-FP-CIT SPECT imaging. We assessed sex differences in the dopaminergic activity of the nigrostriatal and mesolimbic systems using regional-based and voxel-wise analyses of 123 I-FP-CIT binding. We tested whether sex-specific binding alterations would also pertain to the serotoninergic and noradrenergic systems by applying spatial correlation analyses. We applied molecular connectivity analyses to assess potential sex differences in the dopaminergic pathways. Results We found comparable 123 I-FP-CIT binding decreases in the striatum for pDLB males and females compared to controls. However, pDLB females showed lower binding in the extrastriatal projections of the nigrostriatal and mesolimbic dopaminergic systems compared to pDLB males. According to the spatial correlation analysis, sex-specific molecular alterations were also associated with serotonergic and noradrenergic systems. Nigrostriatal and mesolimbic systems’ connectivity was impaired in both groups, with males showing local alterations and females presenting long-distance disconnections between subcortical and cortical regions. Conclusions Sex-specific differences in 123 I-FP-CIT binding were found in our cohort, namely, a trend for lower 123 I-FP-CIT binding in females, significant in the presence of a pDLB diagnosis. pDLB females showed also different patterns of connectivity compared to males, mostly involving extrastriatal regions. 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No research evidence is available on sex differences regarding molecular neurotransmission. This study aimed to assess whether sex can influence neurotransmitter systems in patients with probable DLB (pDLB). Methods We included 123 pDLB patients (male/female: 77/46) and 78 control subjects (male/female: 34/44) for comparison, who underwent 123 I-FP-CIT SPECT imaging. We assessed sex differences in the dopaminergic activity of the nigrostriatal and mesolimbic systems using regional-based and voxel-wise analyses of 123 I-FP-CIT binding. We tested whether sex-specific binding alterations would also pertain to the serotoninergic and noradrenergic systems by applying spatial correlation analyses. We applied molecular connectivity analyses to assess potential sex differences in the dopaminergic pathways. Results We found comparable 123 I-FP-CIT binding decreases in the striatum for pDLB males and females compared to controls. However, pDLB females showed lower binding in the extrastriatal projections of the nigrostriatal and mesolimbic dopaminergic systems compared to pDLB males. According to the spatial correlation analysis, sex-specific molecular alterations were also associated with serotonergic and noradrenergic systems. Nigrostriatal and mesolimbic systems’ connectivity was impaired in both groups, with males showing local alterations and females presenting long-distance disconnections between subcortical and cortical regions. Conclusions Sex-specific differences in 123 I-FP-CIT binding were found in our cohort, namely, a trend for lower 123 I-FP-CIT binding in females, significant in the presence of a pDLB diagnosis. pDLB females showed also different patterns of connectivity compared to males, mostly involving extrastriatal regions. 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subjects Alzheimer's disease
Binding
Cardiology
Correlation analysis
Dementia
Dementia disorders
Dopamine receptors
Female
Females
Gender differences
Heterogeneity
Humans
Imaging
Lewy bodies
Lewy Body Disease - diagnostic imaging
Male
Males
Medical imaging
Medicine
Medicine & Public Health
Mesolimbic system
Neostriatum
Neural networks
Neurodegenerative diseases
Neurology
Neurotransmission
Norepinephrine
Nuclear Medicine
Oncology
Original
Original Article
Orthopedics
Pathology
Radiology
Sex Characteristics
Sex differences
Single photon emission computed tomography
Synuclein
Tomography, Emission-Computed, Single-Photon - methods
Tropanes
title Sex differences in dementia with Lewy bodies: an imaging study of neurotransmission pathways
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